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Cell Therapy Process Development Scientist Jobs in Raleigh, NC

AskBio

Process Engineer II

Durham, NC · On-site

Pioneering science to create transformative molecular medicines. Our mission: Lead innovative ... small-scale gene therapy processes from Process Development into the MSAT laboratory and ...

AskBio

Process Engineer II

Durham, NC · On-site

Pioneering science to create transformative molecular medicines. Our mission: Lead innovative ... small-scale gene therapy processes from Process Development into the MSAT laboratory and ...

Beam Therapeutics

Manufacturing Associate II

Durham, NC · On-site

$80K - $115K/yr

Qualifications: * BS/MS in Life Sciences or Engineering a plus with minimum of 4-6 years of relevant experience. * Experience in SAP, Veeva, and Cell Therapy operations strongly preferred.

NCBiotech

Principal Engineer, MS&T

Durham, NC · On-site

$126K - $234K/yr

... scientific and technical leader for upstream processes, bringing deep expertise in gene therapy ... Leverage deep expertise in upstream manufacturing processes (including mammalian cell culture and ...

Novartis

Principal Engineer, MS&T

Durham, NC

$126K - $234K/yr

... scientific and technical leader for upstream processes, bringing deep expertise in gene therapy ... Leverage deep expertise in upstream manufacturing processes (including mammalian cell culture and ...

Novartis Group Companies

Principal Engineer, MS&T

Durham, NC · On-site

$126K - $234K/yr

... scientific and technical leader for upstream processes, bringing deep expertise in gene therapy ... Leverage deep expertise in upstream manufacturing processes (including mammalian cell culture and ...

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All JobsCell Therapy Process Development Scientist JobsCell Therapy Process Development Scientist Jobs in Raleigh, NC

Cell Therapy Process Development Scientist information

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$18

$34

$49

How much do cell therapy process development scientist jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for cell therapy process development scientist in Raleigh, NC is $34.52, according to ZipRecruiter salary data. Most workers in this role earn between $28.27 and $39.28 per hour, depending on experience, location, and employer.

What is the difference between Cell Therapy Process Development Scientist vs Cell Manufacturing Associate?

AspectCell Therapy Process Development ScientistCell Manufacturing Associate
CredentialsTypically requires a Master's or PhD in biology, biochemistry, or related fieldsUsually holds a Bachelor's degree in life sciences or related areas
Work EnvironmentResearch labs, process development facilities, R&D settingsManufacturing floors, production facilities, GMP environments
Industry UsageDesigning and optimizing cell therapy processes, early-stage developmentExecuting manufacturing protocols, batch production, quality control

The Cell Therapy Process Development Scientist focuses on developing and refining cell therapy processes in research and development settings, often requiring advanced degrees. In contrast, the Cell Manufacturing Associate works primarily on executing manufacturing procedures in GMP environments, typically with a bachelor's degree. Both roles are essential in the cell therapy industry but differ in responsibilities, work environment, and required qualifications.

What are popular job titles related to Cell Therapy Process Development Scientist jobs in Raleigh, NC?

For Cell Therapy Process Development Scientist jobs in Raleigh, NC, the most frequently searched job titles are:

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The top searched job categories for Cell Therapy Process Development Scientist jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Cell Therapy Process Development Scientist jobs?

Cities near Raleigh, NC with the most Cell Therapy Process Development Scientist job openings:

Cell Therapy Process Development Scientist jobs near you
Infographic showing various Cell Therapy Process Development Scientist job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $71,804 per year, or $34.5 per hour.

Downstream Manufacturing Specialist

Morrisville, NC • On-site

Astrix Inc
Recruiting and Staffing Services • 1 - 5K employees
Learn more about Astrix Incexternal

$40 - $42/hr

Contractor, Other

Posted 18 days ago

Key responsibilities

  • Execute downstream manufacturing activities for gene therapy products in accordance with approved batch records, SOPs, protocols, and GMP requirements.

  • Perform and support downstream purification and processing operations, including clarification, filtration, centrifugation, chromatography, TFF, buffer and media preparation, ultrafiltration/diafiltration, product concentration and formulation, aseptic processing, and final bulk operations.

  • Operate, clean, sanitize, and maintain manufacturing equipment and associated systems, and document manufacturing activities accurately in batch records, logbooks, and electronic systems.

Job description

Pay Rate Low: 40 | Pay Rate High: 42
We are seeking a Downstream Manufacturing Specialist to support the manufacturing of gene therapy products in a GMP-regulated environment. This role will be responsible for executing and supporting downstream purification and processing activities, ensuring manufacturing operations are performed safely, efficiently, and in accordance with approved procedures and regulatory requirements.
The ideal candidate has hands-on experience with downstream bioprocessing, strong attention to detail, and a working knowledge of GMP manufacturing practices. This is a contract-to-hire opportunity for an individual who is interested in building a long-term career within a growing gene therapy organization.
Pay rate: $40-42/hr
Shift: 1st shift, with occasional 2nd shift
Key Responsibilities
  • Execute downstream manufacturing activities for gene therapy products in accordance with approved batch records, SOPs, protocols, and GMP requirements.
  • Perform and support downstream purification and processing operations, which may include:
    • Clarification and filtration
    • Centrifugation
    • Chromatography
    • Tangential flow filtration (TFF)
    • Buffer and media preparation
    • Ultrafiltration/diafiltration
    • Product concentration and formulation
    • Aseptic processing and final bulk operations
  • Operate, clean, sanitize, and maintain manufacturing equipment and associated systems.
  • Perform in-process sampling and coordinate with Quality Control for testing as required.
  • Accurately document manufacturing activities in batch records, logbooks, and electronic systems in accordance with Good Documentation Practices (GDP).
  • Identify process deviations, equipment issues, and manufacturing abnormalities and promptly escalate them to appropriate personnel.
  • Support deviation investigations, CAPAs, change controls, and other manufacturing quality initiatives.
  • Follow all applicable GMP, environmental health and safety (EHS), biosafety, and facility procedures.
  • Assist with equipment setup, line clearance, cleaning verification, and manufacturing area preparation.
  • Participate in process optimization, continuous improvement, and manufacturing scale-up activities.
  • Work closely with Manufacturing, Process Development, Quality Assurance, Quality Control, Engineering, and Facilities teams.
  • Support technology transfer and process validation activities as needed.
  • Maintain a clean, organized, and compliant manufacturing environment.
  • Participate in shift activities, overtime, and occasional weekend work based on manufacturing schedules.

Qualifications
Required
  • Bachelor's degree in Biology, Biochemistry, Chemical Engineering, Biotechnology, or a related scientific/engineering discipline, or equivalent relevant experience.
  • 2+ years of experience in biopharmaceutical, biologics, cell therapy, gene therapy, or related GMP manufacturing.
  • Hands-on experience with downstream bioprocessing and purification operations.
  • Understanding of GMP manufacturing principles and Good Documentation Practices.
  • Ability to follow detailed SOPs and batch records while maintaining a high level of accuracy.
  • Strong communication, organizational, and problem-solving skills.
  • Ability to work effectively in a cross-functional, team-oriented environment.
  • Ability to work on-site in a manufacturing environment and wear required PPE.

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